# K102541: Cynosure Cellulaze Laser

- Pathway: 510(k) (Traditional)
- Applicant: Cynosure, Inc.
- Decided: Jan 26, 2012 after 510 days
- Product code: OYW (Laser, Cellulite Appearance)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K091537 (2009). 1 ancestor in all.
39 later devices descend from it; 2 cite it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091537: Cynosure Smartlipo Multiwavelength Laser with 1440NM Wavelength, Cynosure, Inc. (2009) Summary page 1.

## Most influential descendants
- K121127: Sidelaze Laser Beam Delivery Accessory for Cynosure 1440NM Wavelength Lasers (2012), 25 descendants of its own
- K124003: Med-Fibers Surgical Laser Fiber, Med-Fibers Endo-Ent Laser Probes, Med-Fibers End- and Aspirating Laser Probes, Med-Fibe (2013), 23 descendants of its own
- K170366: Laser Peripherals, LLC Family of Bare Laser Fibers (2017), 13 descendants of its own
- K201801: Rapid Acoustic Pulse Device (2021), 12 descendants of its own
- K223237: SofWave System (2022), 7 descendants of its own

## Indications for use
The Cynosure Cellulaze Laser is intended for the short term improvement in the appearance of cellulite.

Source page: https://510kreport.com/device/K102541
Methodology: https://510kreport.com/methodology